POWRE: Research and Career Enhancement Activities to Support Studies in Eukaryotic Ribosomal RNA Maturation

叶片组织中相蛋白启动子TATA区域上的一个旋转和翻译定位的核小体赋予了一种转录无活性的染色质结构。过渡到转录胜任状态需要两个主要步骤：染色质增强和aba介导的激活。在这个项目中，这些步骤所涉及的过程将通过以下具体目标进行更详细的研究：(1)研究pvalf介导的相启动子染色质增强所涉及的机制；(2)确定PvALF结构域在转录激活中的作用；(3)组合顺式元件相互作用及其在aba介导的相启动子激活中的作用的研究。在目的(1)中，在DNA复制抑制剂存在和不存在的情况下，将使用分裂和非分裂组织来研究DNA复制对相激活的影响。一个诱导启动子将用于评估DNA复制对PvALF在分别具有活跃或无DNA复制的幼叶或老叶细胞中增强转录能力的影响。其他用于探索相启动子增强和激活的系统包括在存在和不存在植物核因子（包括天然和修饰的PvALF）的情况下由爪蟾提取物制成的人工核。在目标(2)中，PvALF的A和B2结构域在转录激活中的作用将通过体外和体内方法进行评估。在营养组织和种子组织中，我们将利用携带相启动子RY元件突变和含有（或缺乏）PvALF的等基因系来评估PvALF与特定RY元件的相互作用。DNase I和DMS足迹将在体内进行，以确定这些细胞系组织中的相启动子染色质结构和因子占用。目标(3)中的实验将允许评估RY元件与相邻元件相互作用以产生功能性转录因子组合的能力。其他阶段启动子结构将用于探索特定序列元件在aba介导的转录激活中的参与。相启动子是一种驱动强而严格的组织（种子）特异性基因表达的启动子，被证明在植物生物技术中有着广泛的应用。因此，该项目的研究结果将具有实际应用价值，并为研究转录的基本生物学过程提供一个植物系统。证实复制参与转录激活将是一项重大的科学进步，因为迄今为止还没有人令人信服地说明复制直接参与高级真核生物基因的转录。

Hall NSF project: Chromatin potentiation and ABA activation of phaseolin transcription A rotationally and translationally-positioned nucleosome over the TATA region of the phaseolin (phas) promoter in leaf tissue confers a transcriptionally inactive chromatin structure. Transition to a transcriptionally competent status requires two major steps: chromatin potentiation and ABA-mediated activation. In this project, the processes involved in these steps will be examined in greater detail through the following specific objectives: (1) An investigation of the mechanisms involved in PvALF-mediated chromatin potentiation of the phas promoter; (2) A determination of the role of PvALF domains in transcriptional activation; (3) An examination of combinatorial cis-element interactions and their role in ABA-mediated activation of the phas promoter. In objective (1), the effect of DNA replication on phas activation will be investigated using dividing and non-dividing tissues, in the presence and absence of DNA replication inhibitors. An inducible promoter will be used to evaluate the effect of DNA replication on PvALF's ability to potentiate transcription in cells of young or old leaves which have, respectively, active or no DNA replication. Other systems to be used for exploration of phas promoter potentiation and activation include artificial nuclei made from Xenopus extracts in the presence and absence of plant nuclear factors (including native and modified PvALF). In objective (2), the role of the A and B2 domains of PvALF in transcriptional activation will be evaluated using both in vitro and in vivo approaches. The interaction of PvALF with specific RY elements will be evaluated in vegetative tissues and in seed tissues using isogenic lines bearing phas promoter RY element mutations and containing (or lacking) PvALF. DNase I and DMS footprinting will be undertaken in vivo to determine phas promoter chromatin structure and factor occupancy in tissues of these lines. Experiments in objective (3) will permit evaluation of the ability of RY elements to interact with adjacent elements to yield functional transcription factor combinations. Additional phas promoter constructs will be used to explore the participation of specific sequence elements in ABA-mediated transcriptional activation.The phas promoter, which drives strong and rigorously tissue- (seed) specific gene expression, is proving to be widely used in plant biotechnology. Therefore, findings from this project will have practical application as well as providing a plant system for studying the fundamental biological process of transcription. Confirmation of the participation of replication in transcriptional activation would represent a major scientific advance since no one has thus far illustrated convincingly that replication is directly involved in the transcription of a higher eukaryote gene.